This paper presents a new volume visualization approach for three-dimensional (3-D) interactive microscopy data exploration. Because of their unique image characteristics, 3-D microscopy data are often not able to be visualized effectively by conventional volume visualization techniques. In our approach, microscopy visualization is carried out in an interactive data exploration environment, based on a combination of interactive volume rendering techniques and image-based transfer function design methods. Interactive volume rendering is achieved by using two-dimensional (2-D) texture mapping in a Shear-Warp volume rendering algorithm. Image processing techniques are employed and integrated into the rendering pipeline for the definition and searching of appropriate transfer functions that best reflect the user's visualization intentions. These techniques have been implemented successfully in a prototype visualization system on low-end and middle-range SGI desktop workstations. Since only 2-D texture mapping is required, the system can also be easily ported to PC platforms.

Actins↗

PubMedDate not supplied

Intramucosal nerve cells in human small intestine.

We investigated the intramucosal nerve cells of the human small intestine with histochemical methods to demonstrate nicotinamide adenine dinucleotide diaphorase and acetylcholinesterase and with morphometry. Intramucosal neurons appeared as solitary cells or in small groups, especially in the ileum. Most intramucosal nerve cell bodies were round or oval; some were flat or spindle-shaped. They mostly lay close to the muscularis mucosae, but some were located within the muscularis mucosae and others were some distance away from it. The processes of some mucosal neurons projected towards the submucosa. Most mucosal nerve cells showed acetylcholinesterase activity. The frequency distribution of nerve cell profile areas in the intramucosal cells in the duodenum differed from that of cells in the ileum (P < 0.001). There were more large mucosal nerve cells in the mucosa of the duodenum than in the ileum. There was no significant difference between the frequency distributions of cell profile areas of cells of the mucosa and cells of Meissner's and Henle's plexuses in the same region. We conclude that intramucosal nerve cells, similar to those of the submucosal plexus, exist in the human small intestine. The size of intramucosal nerve cell profiles differs between the duodenum and ileum. This is consistent with their possible different functions.

Acetylcholinesterase↗

PubMedDate not supplied

Distribution of NADPH diaphorase in intramural plexuses of cat and opossum esophagus.

Nonadrenergic noncholinergic (NANC) nerves, releasing nitric oxide (NO), regulate peristalsis in esophageal smooth muscle. The NADPH diaphorase reaction identifies nitric oxide synthase (NOS). NO-synthesizing (NANC) nerves should be more abundant in esophageal smooth muscle than in striated muscle. We used NADPH diaphorase histochemistry in whole-mounts of the esophagus of cat (predominantly striated muscle) and opossum (predominantly smooth muscle) to compare striated and smooth muscle regions. In the opossum myenteric plexus, 90% of nerve cells were stained, with two populations, dark-staining and light-staining cells. Dark cells constituted 35-51% of stained cells with no difference between striated muscle and smooth muscle regions. In the cat myenteric plexus, 50% of cells were unstained in the striated muscle segment, but only 10% in the smooth muscle segment. Stained cells constituted two populations, dark cells and light cells, dark cells making up 48-60% of stained cells in both striated and smooth muscle segments, with no difference between segments. Both dark cells and light cells lay in clusters in opossum, but not in cat. Dark cells showed no selectivity for large or small ganglia of myenteric plexus in either region in opossum. Many more NADPH diaphorase positive nerve fibers lay in the circular smooth muscle layer than in the other layers. They were not found in striated muscle. Interstitial cells of Cajal in the circular layer of smooth muscle were also positive. In the submucosal plexus of opossum, all cells were stained, 10% being dark cells in both striated and smooth muscle segments. The cat has almost no nerve cells in the submucosal plexus. The similarity of the myenteric plexus in striated muscle and smooth muscle regions of the esophagus suggests that NADPH diaphorase positive nerves have other functions besides regulation of smooth muscle. Also, a positive reaction may not dictate that NO is the sole transmitter released.

Animals↗

PubMedDate not supplied

Pneumatocoele and conjunctivitis in a newborn.

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Conjunctivitis, Bacterial↗

PubMedDate not supplied

Immunogenicity of Plasmodium falciparum and Plasmodium vivax circumsporozoite protein repeat multiple antigen constructs (MAC).

In this study we characterized the immunogenic properties of three different multispecies multiple antigen constructs (MACs) carrying the circumsporozoite protein (CSP) repeats of human malaria parasites, Plasmodium falciparum and P. vivax. We synthesized tetrameric MACs containing the antigenic repeats from the CSP of P. vivax-like parasite in two arms and CSP repeat sequences of either P. vivax type-1 (vivax-like/vivax type-1 MAC), P. vivax type-2 (vivax-like/vivax type-2 MAC), or P. falciparum (vivax-like/falciparum MAC) in the other two arms. Mice of four different genetic backgrounds (H-2a, H-2b, H-2d, and H-2k) were immunized with these MACs in Freund's adjuvant. All three MAC preparations were found to elicit antibodies to P. vivax-like CSP repeats in B10.BR, B10.A, and C57BL/6 mice. On the other hand, in B10.D2 mice only vivax-like/vivax type-1 MAC, but not the other two MACs induced antibodies to the P. vivax-like CSP repeats. In mice immunized with vivax-like/vivax type-1 MAC, antibodies to P. vivax type-1 CS repeat peptides were induced in B10.BR, B10.A, and C57BL/6 mice, but not in B10.D2 mice. Antibody responses to P. vivax type-2 repeats were not induced in any of the four strains of mice that were immunized with vivax-like/vivax type-2 MAC. While B10.BR, B10.A, and C57BL/6 mice produced antibodies to NANP repeats of P. falciparum CSP following immunization with vivax-like/falciparum MAC, B10.D2 mice failed to elicit antibodies to this repeat. All the sera that showed positive reactivity to peptides in enzyme-linked immunosorbent assay were found to react with sporozoites by IFA. In conclusion, these results showed that naturally immunogenic epitopes from different species of malaria parasites can be incorporated in a single vaccine construct to induce immune responses against multiple epitopes.

Amino Acid Sequence↗